- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT03717896
당뇨병성 케톤산증에 대한 보조 요법으로서의 티아민
연구 개요
상세 설명
티아민(비타민 B1)은 호기성 포도당 대사에서 중요한 역할을 하는 수용성 비타민입니다. 티아민은 호기성 대사를 위해 크렙스 회로에 진입하기 위해 활성화되어야 하는 효소인 피루브산 탈수소효소(PDH)의 보조인자입니다. PDH 활성은 티아민 결핍 상태에서 감소되어 피루브산 대사가 혐기성 경로로 이동합니다. 이것은 증가된 젖산 생성과 산증을 유발합니다. 결과적으로 티아민 결핍으로 인한 소변의 티아민 손실은 당뇨병에서 드문 일이 아닙니다. 조사관의 예비 연구에 따르면 DKA 환자의 39%에서 티아민 결핍이 발생하고 티아민 수치는 젖산 및 산증과 반비례 관계가 있는 것으로 나타났습니다. 연구원은 DKA 환자를 정맥 티아민으로 치료하면 산증이 더 빨리 해결되고 호기성 대사가 개선될 것이라고 가정합니다. 연구자의 2차 가설은 티아민 치료가 ICU 및 병원에서의 체류를 단축하고 더 적은 병원 자원의 활용으로 이어질 것이라는 것입니다.
이 무작위, 이중 맹검, 위약 대조 시험에서 연구에 등록된 DKA로 병원에 입원한 환자는 무작위로 2일 동안 1일 2회 티아민(0.9% 식염수에 200mg) 또는 동일한 양의 티아민을 투여받게 됩니다. 동일한 일정에 0.9% 식염수. 연구자의 주요 결과는 선형 혼합 효과 모델을 사용하여 0, 6, 12, 18, 24시간에서 측정하여 등록 후 24시간 동안 중탄산염의 변화입니다. 두 번째로, 환자는 유형 I 및 유형 II DM으로 계층화됩니다. 또한, 티아민 결핍 피험자의 사전 계획된 하위 분석이 수행됩니다.
연구 유형
등록 (실제)
단계
- 2 단계
연락처 및 위치
연구 장소
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Massachusetts
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Boston, Massachusetts, 미국, 02215
- Beth Israel Deaconess Medical Center
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
설명
포함 기준:
- 중탄산염 ≤15mEq/L
- 음이온 갭 > 12mEq/L
- 혈액 pH≤ 7.24(임상 팀에서 이미 얻은 경우)
- 소변 케톤(질적) 또는 혈청 케톤(β-하이드록시부티르산) > 3mmol/L
- 발표 후 6시간 이내 등록
제외 기준:
- 현재 티아민 보충 ≥ 하루 6밀리그램(즉, 종합 비타민제 이상)
- 발작, 일산화탄소 중독, 시안화물 독성, 심정지, 간 기능 장애(특히 알려진 간경변으로 정의됨)를 포함한 심각한 산증의 경쟁 원인
- 티아민에 대한 알려진 알레르기
- 임상 팀이 판단한 티아민 투여에 대한 경쟁 적응증(예: 알코올 중독자)
- 연구 보호 인구(임산부, 수감자, 지적 장애인)
- 이전에 동일한 연구에 등록한 환자
- Do Not Resuscitate/Do Not Intubate(DNR/DNI) 또는 Comfort Measures Only(CMO) 코드 상태
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: 티아민
2일 동안 1일 2회 0.9% 식염수 50mL에 200mg IV 티아민
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2일 동안 12시간마다 티아민 200mg IV
다른 이름들:
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위약 비교기: 위약
100mL 0.9% 식염수 1일 2회 이틀 동안
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50mL 0.9% 식염수
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Plasma Bicarbonate Levels
기간: 6, 12, 18, and 24 hours after enrollment
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Primary outcome of plasma bicarbonate levels over 24 hours (6, 12, 18, 24 hours) following enrollment
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6, 12, 18, and 24 hours after enrollment
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Lactate
기간: 6, 12, 18, and 24 hours after enrollment
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Secondary outcome of lactate over 24 hours (6, 12, 18, 24 hours) following enrollment
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6, 12, 18, and 24 hours after enrollment
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Anion Gap
기간: 6, 12, 18, and 24 hours after enrollment
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Secondary outcome of anion gap over 24 hours (6, 12, 18, 24 hours) following enrollment
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6, 12, 18, and 24 hours after enrollment
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ICU Length of Stay
기간: 45 days
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ICU length of stay reflects the number of ICU admission days.
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45 days
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Hospital Length of Stay
기간: 45 days
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Hospital length of stay reflects how long it takes a diabetic ketoacidosis patient to recover to the point where he/she can be released from the hospital.
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45 days
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Duration of Insulin Therapy
기간: First 7 days after enrollment
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The duration of insulin therapy is calculated by examining the hospital clinical information systems for all records of IV insulin infusion beginning at the time of enrollment.
The start and the stop time-stamps of medication infusion are used to calculate a duration of infusion.
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First 7 days after enrollment
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SOFA Score (Sequential Organ Failure Assessement Score)
기간: 24 hours
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The SOFA score is a validated measure of organ dysfunction commonly used in critically ill patients, particularly those with sepsis.
It evaluates the function of six organ systems-respiratory, cardiovascular, neurologic, hepatic, renal, and coagulation-based on routinely collected clinical and laboratory data.
Each organ system is assigned a score from 0 (normal function) to 4 (most severe dysfunction), resulting in a total score ranging from 0 to 24.
Higher SOFA scores indicate greater severity of organ failure and a higher risk of adverse outcomes.
SOFA score in this study uses a modification in which the arterial oxygen saturation/fraction of inspired oxygen (SaO2 /FiO2) ratio is substituted for the partial pressure of arterial oxygen/fraction of inspired oxygen (PaO2 /FiO2 ratio).
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24 hours
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Oxygen Consumption by Circulating Mononuclear Cells
기간: 24 hours
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Oxygen consumption rate of circulating peripheral blood mononuclear cells measured using Seahorse.
Basal respiration represents oxygen consumption under baseline conditions.
ATP-linked respiration represents oxygen consumption coupled to ATP production, while proton leak represents oxygen consumption not linked to ATP synthesis.
Maximal respiration represents the maximal capacity of the electron transport chain after uncoupling.
Spare respiratory capacity represents the difference between maximal and basal respiration and indicates the ability to respond to increased energy demand.
Non-mitochondrial respiration represents oxygen consumption independent of mitochondrial activity.
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24 hours
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Pyruvate Dehydrogenase Activity
기간: 24 hours and 72 hours (or at discharge if hostpial length of stay was less than 72 hours)
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Secondary outcome of change in PDH specific activity over 72 hours or at discharge if patient's hospital length of stay was less than 72 hours.
PDH activity and total PDH protein quantity were measured in isolated peripheral blood mononuclear cells (PBMCs) following selective disruption of the mitochondrial membrane, using a previously validated immunocapture and microplate-based enzymatic assay protocol.
PDH-specific activity was calculated as the ratio of measured PDH enzymatic activity to the natural logarithm of PDH protein quantity (PDH activity / ln[PDH quantity]), providing a normalized metric that reflects the functional efficiency of the enzyme independent of its expression level.
Higher values suggest higher enzymatic efficiency.
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24 hours and 72 hours (or at discharge if hostpial length of stay was less than 72 hours)
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Neurocognitive: Hopkins Verbal Learning Test - Total Recall
기간: At hospital discharge, median of 4 days
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The Hopkins Verbal Learning Test-Revised (HVLT-R) Total Recall score is a measure of verbal learning and immediate memory.
Participants are read a list of 12 words (from three semantic categories) and asked to recall as many words as possible across three consecutive learning trials.
The Total Recall score is calculated as the sum of correctly recalled words across the three trials, yielding a possible range of 0 to 36, with higher scores indicating better verbal learning and memory performance.
This score reflects both initial acquisition and short-term retention of verbal information and is commonly used to assess cognitive function in clinical research.
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At hospital discharge, median of 4 days
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Neurocognitive: Hopkins Verbal Learning Test - Delayed Recall
기간: At hospital discharge, median of 4 days
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The Hopkins Verbal Learning Test-Revised (HVLT-R) Delayed Recall score assesses retention of verbal information after a delay.
Following completion of the three learning trials, participants are asked to recall the previously presented word list after a delay period (typically 20-25 minutes) without re-exposure to the words.
The Delayed Recall score is calculated as the number of correctly recalled words, with a possible range of 0 to 12, where higher scores indicate better memory retention.
This measure reflects the ability to consolidate and retrieve learned information over time and is commonly used to evaluate memory function in clinical and research settings.
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At hospital discharge, median of 4 days
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Neurocognitive: Hopkins Verbal Learning Test - Retention
기간: At hospital discharge, median of 4 days
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The Hopkins Verbal Learning Test-Revised (HVLT-R) Retention (%) score reflects the proportion of learned information that is retained over a delay.
It is calculated as the ratio of the Delayed Recall score to the highest number of words recalled on any of the three immediate recall trials, multiplied by 100, yielding a percentage value.
Scores typically range from 0% to 100%, with higher values indicating better retention of previously learned material.
This measure provides an index of memory retention independent of initial learning performance.
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At hospital discharge, median of 4 days
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Neurocognitive: Hopkins Verbal Learning Test - Recognition Discrimination Index
기간: At hospital discharge, median of 4 days
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The Hopkins Verbal Learning Test-Revised (HVLT-R) Recognition Discrimination Index assesses recognition memory by evaluating the ability to distinguish previously learned words from novel distractors.
During the recognition phase, participants are presented with a list of target words and distractor words and asked to identify those that were previously learned.
The Recognition Discrimination Index is calculated as the number of true positives (correctly identified target words) minus the number of false positives (incorrectly identified distractor words), yielding a score typically ranging from -12 to 12. Higher scores indicate better recognition accuracy and discrimination ability, reflecting the integrity of memory retrieval processes.
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At hospital discharge, median of 4 days
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Neurocognitive: Brief Visuospatial Memory Test
기간: At hospital discharge, median of 4 days
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The Brief Visuospatial Memory Test (BVMT) assesses visuospatial learning and memory.
Participants are shown six geometric designs for a brief period and asked to reproduce them from memory across three learning trials.
Performance is scored based on the accuracy and placement of each design, with a total recall score ranging from 0 to 36, where higher scores indicate better visuospatial memory.
A delayed recall trial is administered after a delay to assess retention of visual information.
This measure evaluates the ability to encode, store, and retrieve visuospatial material.
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At hospital discharge, median of 4 days
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Neurocognitive: Trail Making Test - Test Part A
기간: At hospital discharge, median of 4 days
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The Trail Making Test Part A (TMT-A) assesses visual attention, processing speed, and psychomotor function.
Participants are instructed to connect numbered circles in sequential order as quickly as possible.
The primary outcome is the time to completion, measured in seconds, with lower times indicating better performance.
There is no fixed maximum score, although testing is typically discontinued at a predefined time limit (commonly 300 seconds).
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At hospital discharge, median of 4 days
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Neurocognitive: Trail Making Test - Test Part B
기간: At hospital discharge, median of 4 days
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The Trail Making Test Part B (TMT-B) assesses executive function, including cognitive flexibility and set-shifting, in addition to processing speed.
Participants are required to alternate between numbers and letters in sequence (e.g., 1-A-2-B) as quickly as possible.
The primary outcome is the time to completion, measured in seconds, with lower times indicating better performance.
As with TMT-A, there is no fixed maximum score, and testing is typically discontinued at a predefined time limit (commonly 300 seconds).
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At hospital discharge, median of 4 days
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Neurocognitive: WAIS-IV Digit Span
기간: At hospital discharge, median of 4 days
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The Wechsler Adult Intelligence Scale-Fourth Edition (WAIS-IV) Digit Span subtest assesses attention, working memory, and concentration.
Participants are asked to repeat sequences of numbers in forward order (Digit Span Forward), reverse order (Digit Span Backward), and ascending order (Digit Span Sequencing).
Scores are based on the total number of correctly recalled sequences, with higher scores indicating better attention and working memory capacity.
The total score ranges from 0 to 48.
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At hospital discharge, median of 4 days
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Neurocognitive: Test of Verbal Fluency and Animal Naming
기간: At hospital discharge, median of 4 days
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The Animal Naming test is a measure of semantic verbal fluency and executive function.
Participants are asked to name as many animals as possible within a fixed time period.
The score is the total number of unique, correct animal names generated, with higher scores indicating better semantic memory retrieval and executive functioning.
Scores range from 0 with no fixed upper limit.
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At hospital discharge, median of 4 days
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Neurocognitive: Test of Premorbid Functioning
기간: At hospital discharge, median of 4 days
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The Test of Premorbid Functioning (TOPF) estimates an individual's baseline cognitive ability prior to illness or injury.
Participants are asked to read aloud a list of irregularly spelled words, and performance is scored based on correct pronunciation.
Scores are used to estimate premorbid intellectual functioning.
Scores range from 0 to 70, with higher scores indicating higher estimated premorbid functioning.
This measure helps contextualize current cognitive performance relative to expected baseline levels.
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At hospital discharge, median of 4 days
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기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
C-peptide Levels
기간: 0, 24 hours, and 72 hours (or at discharge if hospital length of stay was less than 72 hours)
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C-peptide levels measured at time of study drug administration, 24 hours, and at 72 hours (or at discharge if hospital length of stay was less than 72 hours).
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0, 24 hours, and 72 hours (or at discharge if hospital length of stay was less than 72 hours)
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공동 작업자 및 조사자
수사관
- 수석 연구원: Michael Donnino, MD, Beth Israel Deaconess Medical Center
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 2018P000475
- 1R01DK112886-01A1 (미국 NIH 보조금/계약)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
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